chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109216387109216389GT--20GENIChomozygous817254707
6109216449109216450AC26GENIChomozygous817254708
6109216711109216712CG31GENIChomozygous817254709
6109217708109217709GA14GENIChomozygous817254710
6109218078109218079TG14GENIChomozygous817254711
6109218132109218133GA14GENIChomozygous817254712
6109218533109218534TC12GENIChomozygous817254713
6109218971109218972CG14GENIChomozygous817254714
6109219945109219946GA12GENIChomozygous817254715
6109220171109220172AG10GENIChomozygous817254716
6109221479109221480AG16GENIChomozygous817254717
6109224251109224252CT14GENIChomozygous817254718
6109224503109224504CT16GENIChomozygous817254719
6109225632109225633TC19GENIChomozygous817254720
6109225969109225970GC14GENIChomozygous817254721
6109226303109226304G-12GENIChomozygous817254722
6109226869109226870T-13GENIChomozygous817254723
6109227067109227069GA--8GENIChomozygous817254724
6109227384109227385TC18GENIChomozygous817254725
6109227512109227513TA10GENIChomozygous817254726
6109228010109228011GA17GENIChomozygous817254727